Neural Crest Deletion of Dlx3 Leads to Major Dentin Defects through Down-regulation of Dspp-Reference-Cited by-同舟云学术

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Neural Crest Deletion of Dlx3 Leads to Major Dentin Defects through Down-regulation of Dspp

Published:2012-04 Issue:15 Volume:287 Page:12230-12240
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Duverger Olivier,Zah Angela,Isaac Juliane,Sun Hong-Wei,Bartels Anne K.,Lian Jane B.,Berdal Ariane,Hwang Joonsung,Morasso Maria I.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference51 articles.

1. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome;Price;Hum. Mol. Genet.,1998

2. DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes;Nieminen;Cells Tissues Organs,2011

3. DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism;Dong;Am. J. Med. Genet.,2005

4. DLX3 mutation in a new family and its phenotypic variations;Lee;J. Dent. Res.,2008

5. DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome;Wright;Am. J. Med. Genet. A,2008

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